ECSP088841A - BENZOAZEPIN-OXI-ACETIC ACID DERIVATIVES AS RECEPTOR AGONISTS ACTIVATED BY DELTA PEROXISOMA PROLIFERATOR USED TO INCREASE HIGH DENSITY-CHOLESTEROL LIPOPROTEIN, REDUCE LOW DENSITY-COLESTEROL LIPOPROTEIN AND REDESTERU-COLESTEROL - Google Patents
BENZOAZEPIN-OXI-ACETIC ACID DERIVATIVES AS RECEPTOR AGONISTS ACTIVATED BY DELTA PEROXISOMA PROLIFERATOR USED TO INCREASE HIGH DENSITY-CHOLESTEROL LIPOPROTEIN, REDUCE LOW DENSITY-COLESTEROL LIPOPROTEIN AND REDESTERU-COLESTEROLInfo
- Publication number
- ECSP088841A ECSP088841A EC2008008841A ECSP088841A ECSP088841A EC SP088841 A ECSP088841 A EC SP088841A EC 2008008841 A EC2008008841 A EC 2008008841A EC SP088841 A ECSP088841 A EC SP088841A EC SP088841 A ECSP088841 A EC SP088841A
- Authority
- EC
- Ecuador
- Prior art keywords
- colesterol
- lipoprotein
- redesteru
- peroxisoma
- benzoazepin
- Prior art date
Links
- 102000004895 Lipoproteins Human genes 0.000 title 2
- 108090001030 Lipoproteins Proteins 0.000 title 2
- 239000000018 receptor agonist Substances 0.000 title 1
- 229940044601 receptor agonist Drugs 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 208000035150 Hypercholesterolemia Diseases 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000035475 disorder Diseases 0.000 abstract 2
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- 208000002177 Cataract Diseases 0.000 abstract 1
- 208000032928 Dyslipidaemia Diseases 0.000 abstract 1
- 206010020772 Hypertension Diseases 0.000 abstract 1
- 206010068961 Hypo HDL cholesterolaemia Diseases 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 208000017170 Lipid metabolism disease Diseases 0.000 abstract 1
- 208000001145 Metabolic Syndrome Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 abstract 1
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 abstract 1
- 208000017442 Retinal disease Diseases 0.000 abstract 1
- 206010038923 Retinopathy Diseases 0.000 abstract 1
- 206010060755 Type V hyperlipidaemia Diseases 0.000 abstract 1
- 201000010390 abdominal obesity-metabolic syndrome 1 Diseases 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 230000002490 cerebral effect Effects 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 230000002526 effect on cardiovascular system Effects 0.000 abstract 1
- 208000006575 hypertriglyceridemia Diseases 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 208000002551 irritable bowel syndrome Diseases 0.000 abstract 1
- 208000028867 ischemia Diseases 0.000 abstract 1
- 208000017169 kidney disease Diseases 0.000 abstract 1
- 230000004322 lipid homeostasis Effects 0.000 abstract 1
- 230000037356 lipid metabolism Effects 0.000 abstract 1
- 208000011661 metabolic syndrome X Diseases 0.000 abstract 1
- 201000001119 neuropathy Diseases 0.000 abstract 1
- 230000007823 neuropathy Effects 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 208000033808 peripheral neuropathy Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 201000010065 polycystic ovary syndrome Diseases 0.000 abstract 1
- 230000002792 vascular Effects 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/06—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D233/08—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms
- C07D233/12—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D233/16—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A61P3/06—Antihyperlipidemics
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D223/16—Benzazepines; Hydrogenated benzazepines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Reproductive Health (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Child & Adolescent Psychology (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La invención está dirigida a compuestos de la fórmula (I) útiles como agonistas de PPAR; también se describen composiciones farmacéuticas y métodos para tratar una o más condiciones incluyendo, pero sin limitarse a, diabetes, nefropatía, neuropatía, retinopatía, síndrome de ovario policístco, hipertensión, isquemia, accidente vascular cerebral, trastorno intestinal irritable, inflamación, cataratas, enfermedades cardiovasculares, síndrome metabólico X, hiper-LDL-colesterolemia, dislipidemia (incluyendo hipertrigliceridemia, hipercolesterolemia, hiperlipidemia mixta, e hipo-HDL-colesterolemia), aterosclerosis, obesidad y otros trastornos relacionados con el metabolismo de lípidos y complicaciones de homeostasis de energía de los mismos, usando compuestos de la invención.The invention is directed to compounds of the formula (I) useful as PPAR agonists; Pharmaceutical compositions and methods for treating one or more conditions including, but not limited to, diabetes, nephropathy, neuropathy, retinopathy, polycystic ovary syndrome, hypertension, ischemia, cerebral vascular accident, irritable bowel disorder, inflammation, cataracts, diseases are also described. cardiovascular, metabolic syndrome X, hyper-LDL-cholesterolemia, dyslipidemia (including hypertriglyceridemia, hypercholesterolemia, mixed hyperlipidemia, and hypo-HDL-cholesterolemia), atherosclerosis, obesity and other disorders related to lipid metabolism and homeostasis energy complications themselves, using compounds of the invention.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79300106P | 2006-04-18 | 2006-04-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP088841A true ECSP088841A (en) | 2008-11-27 |
Family
ID=38610435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2008008841A ECSP088841A (en) | 2006-04-18 | 2008-10-22 | BENZOAZEPIN-OXI-ACETIC ACID DERIVATIVES AS RECEPTOR AGONISTS ACTIVATED BY DELTA PEROXISOMA PROLIFERATOR USED TO INCREASE HIGH DENSITY-CHOLESTEROL LIPOPROTEIN, REDUCE LOW DENSITY-COLESTEROL LIPOPROTEIN AND REDESTERU-COLESTEROL |
Country Status (29)
| Country | Link |
|---|---|
| US (2) | US7678786B2 (en) |
| EP (1) | EP2010289B1 (en) |
| JP (1) | JP5232771B2 (en) |
| KR (1) | KR101472370B1 (en) |
| CN (1) | CN101479008B (en) |
| AR (1) | AR060489A1 (en) |
| AT (1) | ATE535282T1 (en) |
| AU (1) | AU2007237928B2 (en) |
| BR (1) | BRPI0711695A2 (en) |
| CA (1) | CA2649700C (en) |
| CO (1) | CO6160296A2 (en) |
| CR (1) | CR10447A (en) |
| EA (1) | EA016583B1 (en) |
| EC (1) | ECSP088841A (en) |
| ES (1) | ES2375754T3 (en) |
| GT (1) | GT200800226A (en) |
| HN (1) | HN2008001559A (en) |
| IL (1) | IL194850A (en) |
| JO (1) | JO3444B1 (en) |
| MX (1) | MX2008013534A (en) |
| MY (1) | MY144637A (en) |
| NO (1) | NO344334B1 (en) |
| NZ (1) | NZ571998A (en) |
| PE (1) | PE20080188A1 (en) |
| TW (1) | TWI404712B (en) |
| UA (1) | UA96150C2 (en) |
| UY (1) | UY30288A1 (en) |
| WO (1) | WO2007121432A2 (en) |
| ZA (1) | ZA200809790B (en) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2025674A1 (en) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituted tetra hydro naphthalines, method for their manufacture and their use as drugs |
| EP3090739A1 (en) | 2008-01-04 | 2016-11-09 | Schabar Research Associates LLC | Compositions composed of naproxen sodium and nizatidine |
| WO2009097995A1 (en) * | 2008-02-07 | 2009-08-13 | Sanofi-Aventis | Novel phenyl-substituted imidazolidines, method for the production thereof, medicaments containing said compounds and use thereof |
| BRPI0913291A2 (en) | 2008-05-30 | 2019-01-15 | Takeda Pharmaceuticals Co | compound, prodrug, drug, methods for decreasing protein 4 or treating diabetes in a mammal, and use of the compound |
| WO2011107494A1 (en) | 2010-03-03 | 2011-09-09 | Sanofi | Novel aromatic glycoside derivatives, medicaments containing said compounds, and the use thereof |
| WO2011134468A1 (en) | 2010-04-28 | 2011-11-03 | Leo Pharma A/S | Biaryl phosphodiesterase inhibitors |
| EP2582709B1 (en) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| EP2593447B1 (en) | 2010-07-15 | 2016-08-17 | Bayer Intellectual Property GmbH | 3-pyridyl-heteroarylcarboxamide compounds as pesticides |
| CN103298469A (en) | 2010-08-31 | 2013-09-11 | 首尔大学校产学协力财团 | Use of the fetal reprogramming of a PPAR delta agonist |
| WO2012120054A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012120056A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
| EP2683704B1 (en) | 2011-03-08 | 2014-12-17 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012120055A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2766349B1 (en) | 2011-03-08 | 2016-06-01 | Sanofi | Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2817006A1 (en) | 2012-02-24 | 2014-12-31 | Nestec S.A. | Peltatin for use in the treatment of metabolic disorders |
| WO2013124382A1 (en) | 2012-02-24 | 2013-08-29 | Nestec S.A. | Peltatin for use in the treatment of cardiovascular disorders |
| EP2817007A1 (en) | 2012-02-24 | 2014-12-31 | Nestec S.A. | Peltatin for the treatment of chronic inflammatory disorders |
| US9695137B2 (en) * | 2013-03-14 | 2017-07-04 | The University Of Toledo | Analogs of peroxisome proliferator activated receptor (PPAR) agonists, and methods of using the same |
| WO2016057322A1 (en) * | 2014-10-08 | 2016-04-14 | Salk Institute For Biological Studies | Ppar agonists and methods of use thereof |
| WO2021097034A1 (en) * | 2019-11-14 | 2021-05-20 | Cymabay Therapeutics, Inc. | Seladelpar for use in the treatment of intestinal barrier dysfunction and associated diseases |
| US11324727B2 (en) | 2020-07-15 | 2022-05-10 | Schabar Research Associates, Llc | Unit oral dose compositions composed of naproxen sodium and famotidine for the treatment of acute pain and the reduction of the severity of heartburn and/or the risk of heartburn |
| US12514846B2 (en) | 2020-07-15 | 2026-01-06 | Schabar Research Associates Llc | Unit oral dose compositions composed of ibuprofen or a pharmaceutically acceptable salt thereof and famotidine or a pharmaceutically acceptable salt thereof for the treatment of acute pain and the reduction of the severity and/or risk of heartburn and/or upset stomach |
| JP2023534810A (en) | 2020-07-15 | 2023-08-14 | シャバー リサーチ アソシエイツ エルエルシー | A unit oral dose composition consisting of ibuprofen and famotidine for treating acute pain and reducing the severity and/or risk of heartburn |
Family Cites Families (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2460689C3 (en) * | 1974-12-20 | 1980-06-26 | Klinge Pharma Gmbh & Co, 8000 Muenchen | 13-disubstituted propanol (2) derivatives, process for their preparation and their use as pharmaceuticals |
| US4125732A (en) * | 1977-05-06 | 1978-11-14 | American Cyanamid Company | 2-Aryloxy-2-(phenoxyalkoxy)phenyl acetic acid and esters |
| DE3026924A1 (en) | 1980-07-16 | 1982-02-18 | Klinge Pharma GmbH & Co, 8000 München | 1,3-Di:phenoxy-propan-2-ol derivs. - used as hypolipaemics to reduce tri:glyceride and cholesterol levels in the blood |
| DE3028776A1 (en) | 1980-07-29 | 1982-02-25 | Klinge Pharma GmbH & Co, 8000 München | Hypolipaemic 1,3-di:phenoxy-propanone derivs. - prepd. by oxidn. of hydroxy-propoxy cpds. with di:methyl sulphoxide |
| EP0056172B1 (en) | 1981-01-09 | 1985-04-03 | FISONS plc | Phenoxy- and thiophenoxy compounds, methods for their preparation and pharmaceutical formulations containing them |
| JPS58177934A (en) | 1982-04-13 | 1983-10-18 | Takeda Chem Ind Ltd | Benzoquinone derivative |
| ATE22072T1 (en) | 1982-09-30 | 1986-09-15 | Merck Frosst Canada Inc | LEUKOTRIAN ANTAGONISTS, THEIR PREPARATION AND COMPOSITIONS CONTAINING THEM. |
| US4820867A (en) * | 1983-04-21 | 1989-04-11 | Merck Frosst Canada, Inc. | Phenoxypropoxy halophenylacetic acids as leukotriene antagonists |
| US4513006A (en) * | 1983-09-26 | 1985-04-23 | Mcneil Lab., Inc. | Anticonvulsant sulfamate derivatives |
| JPS61268651A (en) | 1985-05-23 | 1986-11-28 | Takeda Chem Ind Ltd | Phenylacetic acid derivative and production thereof |
| EP0204349A3 (en) * | 1985-06-01 | 1990-01-03 | Dr. Karl Thomae GmbH | Heteroaromatic amine derivatives, medicaments containing them and process for their preparation |
| JPH0714910B2 (en) | 1988-12-13 | 1995-02-22 | 塩野義製薬株式会社 | Stable crystalline salt and thromboxane receptor antagonist containing the same |
| US5487008A (en) * | 1990-04-20 | 1996-01-23 | The Regents Of The University Of Michigan | Method and system for detecting the misfire of a reciprocating internal combustion engine in frequency domain |
| CA2092152A1 (en) * | 1992-03-23 | 1993-09-24 | Azuma Igarashi | Phenoxyacetic acid compounds and medical preparations containing them |
| US5726165A (en) * | 1994-07-29 | 1998-03-10 | Smithkline Beecham P.L.C. | Derivatives of 4-(2-aminoethyl)phenoxymethyl-phosphonic and -phosphinic acid and pharmaceutical and veterinary uses therefor |
| CA2244831A1 (en) | 1996-02-02 | 1997-08-07 | John T. Olson | Method of treating diabetes and related disease states |
| JP2002503202A (en) | 1996-02-02 | 2002-01-29 | メルク エンド カンパニー インコーポレーテッド | Antidiabetic drugs |
| JP3268242B2 (en) | 1996-11-14 | 2002-03-25 | 三共株式会社 | Pharmaceuticals containing fused heterocyclic compounds |
| AU8355998A (en) | 1997-07-24 | 1999-02-16 | Yamanouchi Pharmaceutical Co., Ltd. | Medicinal compositions with cholesterol-lowering effect |
| GB9914977D0 (en) | 1999-06-25 | 1999-08-25 | Glaxo Group Ltd | Chemical compounds |
| GB0031107D0 (en) * | 2000-12-20 | 2001-01-31 | Glaxo Group Ltd | Chemical compounds |
| CN1543451A (en) | 2001-06-07 | 2004-11-03 | Modulator of peroxisome proliferator-activated receptors | |
| EP1414778A1 (en) | 2001-07-30 | 2004-05-06 | Novo Nordisk A/S | Novel vinyl carboxylic acid derivatives and their use as antidiabetics etc. |
| WO2003016291A1 (en) * | 2001-08-10 | 2003-02-27 | Nippon Chemiphar Co., Ltd. | ACTIVATOR FOR PEROXISOME PROLIFERATOR-RESPONSIVE RECEPTOR δ |
| JP2005504778A (en) * | 2001-08-29 | 2005-02-17 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | Oral antidiabetic agent |
| MXPA04003398A (en) * | 2001-10-12 | 2004-11-22 | Nippon Chemiphar Co | Activator for peroxisome proliferator-activated receptor delta. |
| ITRM20020014A1 (en) | 2002-01-15 | 2003-07-15 | Sigma Tau Ind Farmaceuti | DERIVATIVES OF A-PHENYLTHIOCARBOXYL AND A-PHYLYOXYCARBOXYL ACIDS USEFUL FOR THE TREATMENT OF DISEASES THAT RESPOND TO THE ACTIVATION OF |
| JP4383177B2 (en) | 2002-03-01 | 2009-12-16 | スミスクライン ビーチャム コーポレーション | hPPAR activator |
| US6875780B2 (en) * | 2002-04-05 | 2005-04-05 | Warner-Lambert Company | Compounds that modulate PPAR activity and methods for their preparation |
| GB0214149D0 (en) | 2002-06-19 | 2002-07-31 | Glaxo Group Ltd | Chemical compounds |
| CA2499380A1 (en) * | 2002-09-05 | 2004-03-18 | Novo Nordisk A/S | Novel vinyl carboxylic acid derivatives and their therapeutical use |
| DE60332860D1 (en) | 2002-10-28 | 2010-07-15 | High Point Pharmaceuticals Llc | NEW COMPOUNDS SUITABLE FOR THE TREATMENT OF PPARIALLY DISTRIBUTED DISEASES |
| KR20050061562A (en) | 2002-10-28 | 2005-06-22 | 노보 노르디스크 에이/에스 | Novel compounds, their preparation and use |
| JP2006516254A (en) * | 2003-01-06 | 2006-06-29 | イーライ・リリー・アンド・カンパニー | Fused heterocyclic derivatives as PPAR modulators |
| EP1581491A1 (en) * | 2003-01-06 | 2005-10-05 | Eli Lilly And Company | Indole derivatives as ppar modulators |
| PL378110A1 (en) | 2003-02-14 | 2006-03-06 | Biogen Idec Ma Inc. | An expression cassette and vector for transient or stable expression of exogenous molecules |
| PA8594401A1 (en) * | 2003-02-21 | 2004-09-16 | Pfizer | CARBOXILIC ACIDS OF HETEROARILO CONDENSED AS A PPAR AGONIST |
| US7244763B2 (en) * | 2003-04-17 | 2007-07-17 | Warner Lambert Company Llc | Compounds that modulate PPAR activity and methods of preparation |
| US6987118B2 (en) * | 2003-05-21 | 2006-01-17 | Pfizer Inc. | Tetrahydroisoquinoline derivatives as PPAR-alpha activators |
| JP2007502815A (en) * | 2003-08-20 | 2007-02-15 | イーライ リリー アンド カンパニー | PPAR regulator |
| UA87467C2 (en) * | 2003-09-19 | 2009-07-27 | Янссен Фармацевтика Н.В | 4-((PHENOXYALKYL)THIO)PHENOXYACETIC ACID AND ITS ANALOGUES 4-((PHENOXYALKYL)THIO)PHENOXYACETIC ACID AND ITS ANALOGUES |
| CA2539403C (en) * | 2003-09-19 | 2013-11-19 | Janssen Pharmaceutica N.V. | 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs |
| ATE362367T1 (en) * | 2003-10-31 | 2007-06-15 | Janssen Pharmaceutica Nv | PHENOXYACETIC ACID DERIVATIVES AS PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR) DUAL AGONISTS |
| WO2005060958A1 (en) * | 2003-12-19 | 2005-07-07 | Kalypsys, Inc. | (5- (2-phenyl)-thiazol-5-ylmethoxy)-indol-1-yl) -acetic acid derivatives and related compounds as modulators of the human ppar-delta receptor for the treatment of metabolic disorders such as type 2 diabetes |
| ATE461932T1 (en) | 2004-04-21 | 2010-04-15 | Schering Corp | PYRAZOLOÄ4,3-EÜ-1,2,4-TRIAZOLOÄ1,5-CUPYRIMIDINES AS ANTAGONISTS OF THE ADENOSINE A2A RECEPTOR |
| WO2005115384A2 (en) * | 2004-05-25 | 2005-12-08 | Metabolex, Inc. | Bicyclic, substituted triazoles as modulators of ppar and methods of their preparation |
| CN1997619B (en) * | 2004-07-01 | 2010-08-25 | 霍夫曼-拉罗奇有限公司 | Ethynyl containing phenyl derivatives |
| CN101018790A (en) * | 2004-09-11 | 2007-08-15 | 塞诺菲-安万特德国有限公司 | 7-azaindoles and their use as PPAR agonists |
| MY145712A (en) * | 2004-09-15 | 2012-03-30 | Janssen Pharmaceutica Nv | 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs |
| PE20060664A1 (en) | 2004-09-15 | 2006-08-04 | Novartis Ag | BICYCLE AMIDAS AS KINASE INHIBITORS |
| MY147518A (en) * | 2004-09-15 | 2012-12-31 | Janssen Pharmaceutica Nv | 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs |
| JO3006B1 (en) * | 2005-09-14 | 2016-09-05 | Janssen Pharmaceutica Nv | Novel Lysine Salts of 4-((Phenoxy Alkyl)Thio)-Phenoxy Acetic Acid Derivatives |
| AU2007210076A1 (en) * | 2006-01-30 | 2007-08-09 | Irm Llc | Polycyclic 1, 2, 3, 4 -tetrahydro- isoquinoline derivatives and compositions comprising them as PPAR modulators |
| GB0618963D0 (en) * | 2006-09-26 | 2006-11-08 | Ucl Business Plc | Formulations and composites with reactive fillers |
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